Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Jason Charng

Showing results (51-60 of 61) with videos related to

Pageof 7
Sort By:
Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Ophthalmic Genetics|September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathyDanial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Ophthalmic Genetics|February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathyZhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine|July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Clinical & Experimental Ophthalmology|February 27, 2020
Western Australia Atropine for the Treatment of Myopia (WA-ATOM) study: Rationale, methodology and participant baseline characteristicsSamantha S Y Lee, David A Mackey, Gareth Lingham, et al.
Ebiomedicine|April 13, 2023
A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degenerationRosie Clark, Samantha Sze-Yee Lee, Ran Du, et al.
BMJ Open|March 29, 2020
Rationale and protocol for the 7- and 8-year longitudinal assessments of eye health in a cohort of young adults in the Raine StudySamantha Sze-Yee Lee, Gareth Lingham, Seyhan Yazar, et al.
Nature Medicine|December 19, 2018
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defectArtur V Cideciyan, Samuel G Jacobson, Arlene V Drack, et al.
Plos Genetics|October 18, 2021
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|November 1, 2016
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Human Molecular Genetics|October 5, 2018
Variegated yet non-random rod and cone photoreceptor disease patterns in RPGR-ORF15-associated retinal degenerationJason Charng, Artur V Cideciyan, Samuel G Jacobson, et al.
Ophthalmic Genetics|September 28, 2020
Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in <i>PRPF31</i>-associated retinopathyDanial Roshandel, Jennifer A Thompson, Jason Charng, et al.
Ophthalmic Genetics|February 24, 2021
Deep clinical phenotyping and gene expression analysis in a patient with <i>RCBTB1</i>-associated retinopathyZhiqin Huang, Dan Zhang, Jennifer A Thompson, et al.
Molecular Genetics & Genomic Medicine|July 7, 2020
Phenotype-genotype correlations in a pseudodominant Stargardt disease pedigree due to a novel ABCA4 deletion-insertion variant causing a splicing defectDi Huang, Jennifer A Thompson, Jason Charng, et al.
Clinical & Experimental Ophthalmology|February 27, 2020
Western Australia Atropine for the Treatment of Myopia (WA-ATOM) study: Rationale, methodology and participant baseline characteristicsSamantha S Y Lee, David A Mackey, Gareth Lingham, et al.
Ebiomedicine|April 13, 2023
A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degenerationRosie Clark, Samantha Sze-Yee Lee, Ran Du, et al.
BMJ Open|March 29, 2020
Rationale and protocol for the 7- and 8-year longitudinal assessments of eye health in a cohort of young adults in the Raine StudySamantha Sze-Yee Lee, Gareth Lingham, Seyhan Yazar, et al.
Nature Medicine|December 19, 2018
Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defectArtur V Cideciyan, Samuel G Jacobson, Arlene V Drack, et al.
Plos Genetics|October 18, 2021
Correction: Genetic variation affects morphological retinal phenotypes extracted from UK Biobank optical coherence tomography imagesHannah Currant, Pirro Hysi, Tomas W Fitzgerald, et al.
Pageof 7